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rs786203355

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203355(-;-)
Make rs786203355(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position28725323
GeneCHEK2
is asnp
is mentioned by
dbSNPrs786203355
ebirs786203355
HLIrs786203355
Exacrs786203355
Varsomers786203355
Maprs786203355
PheGenIrs786203355
hapmaprs786203355
1000 genomesrs786203355
hgdprs786203355
ensemblrs786203355
gopubmedrs786203355
geneviewrs786203355
scholarrs786203355
googlers786203355
pharmgkbrs786203355
gwascentralrs786203355
openSNPrs786203355
23andMers786203355
23andMe allrs786203355
SNP Nexus

SNPshotrs786203355
SNPdbers786203355
MSV3drs786203355
GWAS Ctlgrs786203355
Max Magnitude0
ClinVar
Risk rs786203355(;)
Alt rs786203355(;)
Reference rs786203355(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000022.10:g.29121311delC
CLNSRC
CLNACC RCV000166630.1,